chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	74721030	74721030		TGCTTGCTAGGCAAGCGCTCTACCACTGAGCTAAATCCCCA	10	GENIC	homozygous	128923623
11	74725224	74725225	G		9	GENIC	homozygous	129989616
11	74725190	74725191	C		9	GENIC	homozygous	129989610
11	74725208	74725209	T		9	GENIC	homozygous	129989611
11	74725210	74725211	T		9	GENIC	homozygous	129989613
11	74725214	74725215	A		9	GENIC	homozygous	129989615
11	74725231	74725232	A		9	GENIC	homozygous	129989618
11	74725250	74725251	G		9	GENIC	homozygous	129989619
11	74725254	74725255	C		9	GENIC	homozygous	129989621
11	74725280	74725280		G	11	GENIC	homozygous	129989622
11	74728480	74728481	T		24	GENIC	homozygous	128923624
11	74728501	74728502	T		19	GENIC	homozygous	128923625
11	74728502	74728503	T	G	19	GENIC	homozygous	123527930
11	74728543	74728543		T	11	GENIC	homozygous	128923626
11	74728569	74728570	A		2	GENIC	homozygous	128923627
11	74728573	74728574	C	T	1	GENIC	homozygous	128944680
11	74728579	74728580	G		1	GENIC	homozygous	130401242
11	74728601	74728601		T	1	GENIC	homozygous	130401243
11	74728609	74728610	C		1	GENIC	homozygous	130401244
11	74728611	74728612	G		1	GENIC	homozygous	130401245
11	74728637	74728638	G		1	GENIC	homozygous	130401246
11	74768654	74768655	G	T	12	GENIC	homozygous	116321888
11	74768660	74768661	A		14	GENIC	homozygous	128923643
11	74768667	74768669	TT		15	GENIC	homozygous	128923644
11	74768677	74768677		G	17	GENIC	homozygous	128923645